Does CODEINE\GUAIFENESIN\PHENIRAMINE Cause Product use issue? 16 Reports in FDA Database
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According to the FDA Adverse Event Reporting System (FAERS), 16 reports of Product use issue have been filed in association with CODEINE\GUAIFENESIN\PHENIRAMINE. This represents 59.3% of all adverse event reports for CODEINE\GUAIFENESIN\PHENIRAMINE.
16
Reports of Product use issue with CODEINE\GUAIFENESIN\PHENIRAMINE
59.3%
of all CODEINE\GUAIFENESIN\PHENIRAMINE reports
16
Deaths
0
Hospitalizations
How Dangerous Is Product use issue From CODEINE\GUAIFENESIN\PHENIRAMINE?
Of the 16 reports, 16 (100.0%) resulted in death.
Is Product use issue Listed in the Official Label?
This adverse event is not currently listed in the official FDA drug label for CODEINE\GUAIFENESIN\PHENIRAMINE. However, 16 reports have been filed with the FAERS database.
What Other Side Effects Does CODEINE\GUAIFENESIN\PHENIRAMINE Cause?
Fatigue (20)
Thrombocytopenia (20)
Asthma (19)
Back pain (19)
Bursitis (19)
Coeliac disease (19)
Constipation (19)
Contraindicated product administered (19)
Drug hypersensitivity (19)
Drug intolerance (19)
What Other Drugs Cause Product use issue?
INFLIXIMAB (12,752)
DUPILUMAB (10,575)
POLYETHYLENE GLYCOL 3350 (9,432)
METHOTREXATE (8,185)
DICLOFENAC (8,009)
RITUXIMAB (6,948)
ADALIMUMAB (6,379)
ETANERCEPT (6,062)
TOCILIZUMAB (5,944)
ABATACEPT (5,915)